This is a non-core endpoint: only basic statistics are computed.
See these related core endpoints for full statistics:
Motor neuron disease (with DMD)
DOID EFO MESH Endpoint Browser
MND
muscular disease: Acquired, familial, and congenital disorders of skeletal muscle and smooth muscle.
Endpoint definition
↥
FinnGen phenotype data
429209 individuals
Apply sex-specific rule None
429209
Check conditions None
429209
Check pre-conditions, main-only, mode, registry filters
2 out of 7 registries used, show all original rules.
26
Check minimum number of events None
26
Remove individuals based on genotype QC
555
MND
Extra metadata
First used in FinnGen datafreeze
DF3
Parent code in ICD-10
G710
Name in latin
Dystrophia musculorum gravis (Duchenne)
Show upset plot detailing case counts by codes
Or the full data table
Similar endpoints
↥List of similar endpoints to
Motor neuron disease (with DMD)
based on the number of shared cases.
Broader endpoints:
Narrower endpoints:
Summary Statistics
↥Key figures
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 555 | 210 | 345 |
| Unadjusted prevalence (%) | 0.13 | 0.09 | 0.19 |
| Mean age at first event (years) | 63.04 | 63.36 | 62.85 |
Mortality
Not a core endpoint, no data to show.
Age distribution of first events
Year distribution of first events
Cumulative Incidence
Not a core endpoint, no data to show.
Correlations
↥
Index endpoint: MND – Motor neuron disease (with DMD)
GWS hits:
Survival analyses between endpoints
↥Not a core endpoint, no data to show.
Drugs most likely to be purchased after Motor neuron disease (with DMD)
↥Endpoint not on priority list, no data to show.